Continuous Illumination of a Conjugated Polymer Causes Strong Enhancement of Photoluminescence.

We present measurements of absorbance and photoluminescence (PL) for films of poly(3-(2,5-dioctylphenyl)thiophene) (PDOPT) as a function of temperature (T) and time (t) of illumination. While having no detectable influence on absorbance of this conjugated polymer, our experiments clearly revealed that illumination of PDOPT caused a significant increase in the PL intensity (IPL(T,t)), that is, the emission probability of PDOPT. Without illumination, we always observed a decrease in IPL with time. An increase in IPL was only detectable when the sample was illuminated. Interestingly, while absorption and emission of photons occur on a time scale of nanoseconds, the here-reported changes in the emission probability were slow and occurred on a time scale of minutes to hours. The influence of illumination on changes in IPL(T,t) was qualitatively similar for slowly and rapidly crystallized PDOPT, that is, the degree of crystallinity was not decisive for the observation. The rate of the increase in IPL depended clearly on the power of the illumination light source. As a function of the illumination time, the change in IPL(T,t) was nonmonotonic and depended on sample temperature. We speculate that changes in polymer interactions caused by excited electronic states might have induced slow changes in polymer conformations.